Investigation of Genetic Diversity of Pasteurella multocida Isolated from Diseased Poultry in Korea

ABSTRACT Pasteurella multocida causes fowl cholera which is an economically important disease in poultry industries around the world. In this study, we analyzed the capsular genotype, lipopolysaccharide (LPS) genotype, virulence-associated genes (VAGs) patterns, antimicrobial resistance and genetic diversity in a total of 9 P. multocida isolates from poultry with fowl cholera between 2014 and 2019 in Korea. When combining the capsular types with the LPS genotypes, two isolates of the 9 isolates were A:L3, and the others were non-typeable (NT): L3. Of the 23 VAGs, all the isolates harbored ptfA, fimA, hsf-1, hsf-2, pfhA, exbB, exbD, tonB, hgbA, hgbB, fur, sodA, sodC, pmHAS, ompA, ompH, oma87, plpB, psl, and nanH, whereas toxA gene was not detected in any of the 9 isolates. In addition, among the 11 antimicrobials, most of the isolates except for one isolate resistant to florfenicol, exhibited susceptibility to all the antimicrobials. Multi-locus sequence typing (MLST) analysis revealed 5 different sequence types (ST): ST8, ST351, ST352, ST353, and ST368. The ST351, ST352, ST353, and ST368 were identified for the first time in this study, and ST352 and ST353 isolates were largely prevalent nationwide. These STs isolates should be monitored continuously because in some cases, ST352 and ST353 isolates demonstrated high mortality rates. Although only limited numbers of isolates have been analyzed, our findings provide overall characteristics and epidemiological information of the P. multocida strains recently prevalent in Korea.

Assessment of FTA card employment for Pasteurella multocida DNA transport and detection of virulence-associated genes in strains isolated from fowl cholera in the United States / Avaliação do emprego de cartões FTA para o transporte do DNA de Pasteurella multocida e pesquisa de genes associados à virulência em cepas isoladas de cólera aviária nos Estados Unidos

Fowl Cholera (FC) is a disease caused by Pasteurella multocida. The severity of this disease is partly caused by virulence factors. Genes encoding fimbriae, capsule, sialidases and proteins for iron metabolism may be related to P. multocida's ability to infect the host. Besides to examining DNA for the presence of virulence genes, DNA is essential for the diagnostic and FTA cards are an alternative for genetic material transport. The study aims to evaluate the viability of P. multocida DNA transport using the cards and to detect 14 virulence genes in 27 strains isolated from FC cases in the United States by multiplex-PCR. No growth was observed in any of the FTA cards, which was essential to assess the security. Furthermore, DNA detection was possible in 100% of the samples, independent of the storage period (7 to 35 days) and temperature (4°C and 37°C). ptfA, exbd-tonB, hgbA, nanB, oma87, hyaD-hyaC, sodC, hgbB, sodA, nanH and pfhA genes were detected in more than 80% of the samples. FTA cards have proven to be a viable and safe tool for DNA transport of P. multocida. A majority of genes showed a high frequency, which was similar to strains isolated from FC cases.(AU)

Cólera aviária (CA) é uma doença causada pela bactéria Pasteurella multocida e a severidade dos casos é em parte justificada por fatores de virulência. Genes codificando fímbrias, cápsulas, sialidases, dismutases e proteínas do metabolismo férrico podem ser relacionados à capacidade do agente em infectar o hospedeiro. Além da obtenção do DNA para pesquisa de genes de virulência, o material genético é fundamental para o diagnóstico, e os cartões FTA seriam uma alternativa no transporte de microrganismos. Os objetivos da presente pesquisa foram avaliar a viabilidade do transporte de DNA de P. multocida através dos cartões e detectar 14 genes de virulência em 27 cepas isoladas de CA nos Estados Unidos, por meio de multiplex-PCR. Nenhuma das amostras para análise microbiológica da segurança dos cartões apresentou crescimento. Foi possível a detecção do DNA em 100% das amostras, independentemente do tempo de estocagem (sete a 35 dias) e das temperaturas (4°C e 37°C) avaliadas. Genes ptfA, exbd-tonB, hgbA, nanB, oma87, hyaD-hyaC, sodC, hgbB, sodA, nanH e pfhA foram detectados em mais de 80% das amostras. Os cartões FTA demonstraram ser uma ferramenta viável e segura para o transporte do DNA de P. multocida. A maioria dos genes apresentou uma alta frequência, compatível com isolados de CA.(AU)

Assessment of FTA card employment for Pasteurella multocida DNA transport and detection of virulence-associated genes in strains isolated from fowl cholera in the United States / Avaliação do emprego de cartões FTA para o transporte do DNA de Pasteurella multocida e pesquisa de genes associados à virulência em cepas isoladas de cólera aviária nos Estados Unidos

Fowl Cholera (FC) is a disease caused by Pasteurella multocida. The severity of this disease is partly caused by virulence factors. Genes encoding fimbriae, capsule, sialidases and proteins for iron metabolism may be related to P. multocida's ability to infect the host. Besides to examining DNA for the presence of virulence genes, DNA is essential for the diagnostic and FTA cards are an alternative for genetic material transport. The study aims to evaluate the viability of P. multocida DNA transport using the cards and to detect 14 virulence genes in 27 strains isolated from FC cases in the United States by multiplex-PCR. No growth was observed in any of the FTA cards, which was essential to assess the security. Furthermore, DNA detection was possible in 100% of the samples, independent of the storage period (7 to 35 days) and temperature (4°C and 37°C). ptfA, exbd-tonB, hgbA, nanB, oma87, hyaD-hyaC, sodC, hgbB, sodA, nanH and pfhA genes were detected in more than 80% of the samples. FTA cards have proven to be a viable and safe tool for DNA transport of P. multocida. A majority of genes showed a high frequency, which was similar to strains isolated from FC cases.(AU)

Cólera aviária (CA) é uma doença causada pela bactéria Pasteurella multocida e a severidade dos casos é em parte justificada por fatores de virulência. Genes codificando fímbrias, cápsulas, sialidases, dismutases e proteínas do metabolismo férrico podem ser relacionados à capacidade do agente em infectar o hospedeiro. Além da obtenção do DNA para pesquisa de genes de virulência, o material genético é fundamental para o diagnóstico, e os cartões FTA seriam uma alternativa no transporte de microrganismos. Os objetivos da presente pesquisa foram avaliar a viabilidade do transporte de DNA de P. multocida através dos cartões e detectar 14 genes de virulência em 27 cepas isoladas de CA nos Estados Unidos, por meio de multiplex-PCR. Nenhuma das amostras para análise microbiológica da segurança dos cartões apresentou crescimento. Foi possível a detecção do DNA em 100% das amostras, independentemente do tempo de estocagem (sete a 35 dias) e das temperaturas (4°C e 37°C) avaliadas. Genes ptfA, exbd-tonB, hgbA, nanB, oma87, hyaD-hyaC, sodC, hgbB, sodA, nanH e pfhA foram detectados em mais de 80% das amostras. Os cartões FTA demonstraram ser uma ferramenta viável e segura para o transporte do DNA de P. multocida. A maioria dos genes apresentou uma alta frequência, compatível com isolados de CA.(AU)

Establishment of a pathogenicity index for mice to Pasteurella multocida strains isolated from poultry and swine

Fowl cholera is a contagious disease that results from infection by the bacterium Pasteurella multocida. This microorganism is extensively distributed among animal species, but little is known regarding its pathogenesis and specificity to various hosts. Many studies using pathogenicity evaluation methods are subjective and difficult to quantify because they are often only involved in the observation of the lethal capacity of the agent in experimental inoculation. Due to a lack of more consistent data, this study aimed to establish a classification model of P. multocida pathogenicity in mice using strains isolated from poultry and swine. A total of 94 strains of P. multocida isolated from clinical cases of FC and from lungs of swine were tested. A volume of 0.1 mL of bacterial suspension was obtained from the concentration of 106 CFU/mL and inoculated by an intraperitoneal route in five mice. The animals were observed every six hours over seven days. In addition to the mortality observed, the time of death and gross lesions were also analyzed. The Pathogenicity Indexes obtained showed significant differences (p<0.05) according to the origin of the strains. Likewise, the number of gross lesions and isolation percentages were also varied (p<0.05) among strains isolated from poultry and swine. From the observed ratios, the isolates were grouped into three pathogenicity classes: high, medium and low. This study proposed a consistent measurement and classification of P. multocida pathogenicity. The obtained results will be used to generate other adjusted models, as well as to form the basis for disease diagnosis.(AU)

Establishment of a pathogenicity index for mice to Pasteurella multocida strains isolated from poultry and swine

Fowl cholera is a contagious disease that results from infection by the bacterium Pasteurella multocida. This microorganism is extensively distributed among animal species, but little is known regarding it’s pathogenesis and specificity to various hosts. Many studies using pathogenicity evaluation methods are subjective and difficult to quantify because they are often only involved in the observation of the lethal capacity of the agent in experimental inoculation. Due to a lack of more consistent data, this study aimed to establish a classification model of P. multocida pathogenicity in mice using strains isolated from poultry and swine. A total of 94 strains of P. multocida isolated from clinical cases of FC and from lungs of swine were tested. A volume of 0.1 mL of bacterial suspension was obtained from the concentration of 106 CFU/mL and inoculated by an intraperitoneal route in five mice. The animals were observed every six hours over seven days. In addition to the mortality observed, the time of death and gross lesions were also analyzed. The Pathogenicity Indexes obtained showed significant differences (p<0.05) according to the origin of the strains. Likewise, the number of gross lesions and isolation percentages were also varied (p<0.05) among strains isolated from poultry and swine. From the observed ratios, the isolates were grouped into three pathogenicity classes: high, medium and low. This study proposed a consistent measurement and classification of P. multocida pathogenicity. The obtained results will be used to generate other adjusted models, as well as to form the basis for disease diagnosis.

Climate Variability and Avian Cholera Transmission in Guangxi, China

In recent years, Guangxi has become one of the most severely affected provinces by epidemics of avian cholera in China. To date, the major determinant climatic factors of the disease in the region have remained largely unknown, making it difficult to effectively target countermeasures for avian cholera surveillance and control. This study aimed to quantify the relationship between climatic variables and cases of avian cholera in subtropical areas of China. Data relating to local meteorological variables and notified cases of avian cholera were supplied by the relevant authorities between January 2006 and December 2015. Spearman correlation, co-linearity statistics and cross-correlation analysis were applied to the data, controlling for co-linearity and lag effects. A time-series Poisson regression analysis was conducted to examine the degree of correlation between the climate variables and avian cholera transmission. The results indicated that monthly mean temperature, relative humidity, rainfall and the multivariate El Niño Southern Oscillation Index, with 2-3 months lag, were correlated with avian cholera incidence. The final model had good predictive ability for the occurrence of avian cholera. Overall, the findings indicate that climate variability plays an important role in avian cholera transmission in Guangxi province. Adoption of the model presented in this study could usefully inform avian cholera surveillance strategies, making them significantly simpler and more effective. The model could also serve as a decision support tool for veterinary professionals and health authorities.(AU)

Climate Variability and Avian Cholera Transmission in Guangxi, China

In recent years, Guangxi has become one of the most severely affected provinces by epidemics of avian cholera in China. To date, the major determinant climatic factors of the disease in the region have remained largely unknown, making it difficult to effectively target countermeasures for avian cholera surveillance and control. This study aimed to quantify the relationship between climatic variables and cases of avian cholera in subtropical areas of China. Data relating to local meteorological variables and notified cases of avian cholera were supplied by the relevant authorities between January 2006 and December 2015. Spearman correlation, co-linearity statistics and cross-correlation analysis were applied to the data, controlling for co-linearity and lag effects. A time-series Poisson regression analysis was conducted to examine the degree of correlation between the climate variables and avian cholera transmission. The results indicated that monthly mean temperature, relative humidity, rainfall and the multivariate El Niño Southern Oscillation Index, with 2-3 months lag, were correlated with avian cholera incidence. The final model had good predictive ability for the occurrence of avian cholera. Overall, the findings indicate that climate variability plays an important role in avian cholera transmission in Guangxi province. Adoption of the model presented in this study could usefully inform avian cholera surveillance strategies, making them significantly simpler and more effective. The model could also serve as a decision support tool for veterinary professionals and health authorities.

Evaluation of the biofilm formation capacity of Pasteurella multocida strains isolated from cases of fowl cholera and swine lungs and its relationship with pathogenicity / Avaliação da capacidade de formação de biofilme por cepas de Pasteurella multocida isoladas de casos de cólera aviária e de pulmões de suínos e sua relação com a patogenicidade

Pasteurella multocida is a Gram-negative bacillus that causes economic losses due to the development of respiratory diseases in several animal species. Among the mechanisms of virulence, the formation of biofilms is an important factor for bacterial survival in hostile environments. Studies of biofilm formation by P. multocida are needed because P. multocida is an important pathogen involved in respiratory infections. However, in contrast to other microorganisms, few studies of biofilm formation have examined P. multocida. Studies comparing the pathogenicity of microbial strains as a function of their biofilm production capacity are also rare. Consequently, the aim of this study was to evaluate the biofilm formation capacity of 94 P. multocida strains isolated from cases of fowl cholera and from swine lungs on polystyrene plates. The associations of the biofilm formation capacity with the pathogenicity index (PI) in vivo and with the presence of four genes (screened by PCR) of the tad locus (tadB, tadD, tadE and tadG), described as adhesion markers, were also determined. Strains from both animal origins were able to form biofilms. However, most of the specimens (52.13%) were classified as weak producers, and more than 40% of the strains of P. multocida (40.42%) did not produce biofilms. There was no significant difference (p>0.05) in the degree of biofilm production between the two sources of isolation. Of the analyzed strains, 56.52% contained all four genes (tadB, tadD, tadE and tadG). The PI arithmetic mean of the strains classified as non-biofilm producers was significantly different (p<0.05) from the PI of moderate-producer strains. The PI of specimens classified as weak biofilm producers also differed significantly (p<0.05) from that of the moderate-producer strains. The results indicate that even though the P. multocida strains isolated from cases of fowl cholera and swine lungs formed biofilms on polystyrene surfaces, adhesion was usually weak. The genes tadB, tadD, tadE and tadG were not significantly associated (p>0.05) with the production of biofilms and with the origin of a given strain. Finally, low virulence strains may suggest a higher biofilm formation capacity on polystyrene plates.(AU)

Pasteurella multocida é um bacilo Gram negativo que ocasiona perdas econômicas, geralmente associadas a doenças respiratórias em diversas espécies animais. Entre os mecanismos de virulência existentes, a formação de biofilmes demonstra ser um importante fator para a proteção e para a sobrevivência bacteriana em ambientes hostis. Estudos relacionados à formação de biofilmes por P. multocida são necessários, uma vez que este é um importante patógeno envolvido em infecções respiratórias. Entretanto, ainda são poucos os estudos desenvolvidos nesta área, quando comparados com aqueles envolvendo outros microrganismos. Também são os raros os estudos que comparam a patogenicidade das cepas com a sua capacidade de produção de biofilme. Neste contexto, o objetivo deste estudo foi avaliar a capacidade de formação de biofilme em placas de poliestireno de 94 cepas de P. multocida isoladas de casos de cólera aviária e de pulmões de suínos, associando-se com o índice de patogenicidade (IP) in vivo e com a presença de quatro genes do locus tad (tadB, tadD, tadE e tadG), descritos como marcadores de adesão e pesquisados através de PCR. As cepas de ambas as origens foram capazes de formar biofilme. Contudo, a maioria dos exemplares (52,12%) foi classificada como fracamente produtora e mais de 40% das cepas de P. multocida (40,42%) não produziram biofilme. Não foi observada diferença estatística (p>0,05) quanto ao grau de produção de biofilme entre as duas origens de isolamento. 56,52% das cepas analisadas apresentaram os quatro genes (tadB, tadD, tadE e tadG) concomitantemente. O IP médio das cepas classificadas como não produtoras de biofilme apresentou diferença estatística (p˂0,05) em relação ao IP das cepas moderadamente produtoras. Os exemplares classificados como fracamente produtores de biofilme diferiram significativamente (p˂0,05) do grupo de cepas moderadamente produtoras. Os resultados obtidos indicaram que, apesar de as cepas de P. multocida isoladas de casos de cólera aviária e do pulmão de suínos apresentarem capacidade de formar biofilme em superfícies de poliestireno, a adesão ocorreu geralmente de forma fraca. Os genes tadB, tadD, tadE e tadG, pertencentes ao locus tad, não apresentaram associação significativa com a produção de biofilme e nem com a origem de isolamento da cepa. Por fim, observou-se que as cepas de menor patogenicidade apresentaram uma maior capacidade de formação de biofilme em placas de poliestireno.(AU)

Evaluation of the biofilm formation capacity of Pasteurella multocida strains isolated from cases of fowl cholera and swine lungs and its relationship with pathogenicity / Avaliação da capacidade de formação de biofilme por cepas de Pasteurella multocida isoladas de casos de cólera aviária e de pulmões de suínos e sua relação com a patogenicidade

Pasteurella multocida is a Gram-negative bacillus that causes economic losses due to the development of respiratory diseases in several animal species. Among the mechanisms of virulence, the formation of biofilms is an important factor for bacterial survival in hostile environments. Studies of biofilm formation by P. multocida are needed because P. multocida is an important pathogen involved in respiratory infections. However, in contrast to other microorganisms, few studies of biofilm formation have examined P. multocida. Studies comparing the pathogenicity of microbial strains as a function of their biofilm production capacity are also rare. Consequently, the aim of this study was to evaluate the biofilm formation capacity of 94 P. multocida strains isolated from cases of fowl cholera and from swine lungs on polystyrene plates. The associations of the biofilm formation capacity with the pathogenicity index (PI) in vivo and with the presence of four genes (screened by PCR) of the tad locus (tadB, tadD, tadE and tadG), described as adhesion markers, were also determined. Strains from both animal origins were able to form biofilms. However, most of the specimens (52.13%) were classified as weak producers, and more than 40% of the strains of P. multocida (40.42%) did not produce biofilms. There was no significant difference (p>0.05) in the degree of biofilm production between the two sources of isolation. Of the analyzed strains, 56.52% contained all four genes (tadB, tadD, tadE and tadG). The PI arithmetic mean of the strains classified as non-biofilm producers was significantly different (p<0.05) from the PI of moderate-producer strains. The PI of specimens classified as weak biofilm producers also differed significantly (p<0.05) from that of the moderate-producer strains. The results indicate that even though the P. multocida strains isolated from cases of fowl cholera and swine lungs formed biofilms on polystyrene surfaces, adhesion was usually weak. The genes tadB, tadD, tadE and tadG were not significantly associated (p>0.05) with the production of biofilms and with the origin of a given strain. Finally, low virulence strains may suggest a higher biofilm formation capacity on polystyrene plates.(AU)

Pasteurella multocida é um bacilo Gram negativo que ocasiona perdas econômicas, geralmente associadas a doenças respiratórias em diversas espécies animais. Entre os mecanismos de virulência existentes, a formação de biofilmes demonstra ser um importante fator para a proteção e para a sobrevivência bacteriana em ambientes hostis. Estudos relacionados à formação de biofilmes por P. multocida são necessários, uma vez que este é um importante patógeno envolvido em infecções respiratórias. Entretanto, ainda são poucos os estudos desenvolvidos nesta área, quando comparados com aqueles envolvendo outros microrganismos. Também são os raros os estudos que comparam a patogenicidade das cepas com a sua capacidade de produção de biofilme. Neste contexto, o objetivo deste estudo foi avaliar a capacidade de formação de biofilme em placas de poliestireno de 94 cepas de P. multocida isoladas de casos de cólera aviária e de pulmões de suínos, associando-se com o índice de patogenicidade (IP) in vivo e com a presença de quatro genes do locus tad (tadB, tadD, tadE e tadG), descritos como marcadores de adesão e pesquisados através de PCR. As cepas de ambas as origens foram capazes de formar biofilme. Contudo, a maioria dos exemplares (52,12%) foi classificada como fracamente produtora e mais de 40% das cepas de P. multocida (40,42%) não produziram biofilme. Não foi observada diferença estatística (p>0,05) quanto ao grau de produção de biofilme entre as duas origens de isolamento. 56,52% das cepas analisadas apresentaram os quatro genes (tadB, tadD, tadE e tadG) concomitantemente. O IP médio das cepas classificadas como não produtoras de biofilme apresentou diferença estatística (p˂0,05) em relação ao IP das cepas moderadamente produtoras. Os exemplares classificados como fracamente produtores de biofilme diferiram significativamente (p˂0,05) do grupo de cepas moderadamente produtoras. Os resultados obtidos indicaram que, apesar de as cepas de P. multocida isoladas de casos de cólera aviária e do pulmão de suínos apresentarem capacidade de formar biofilme em superfícies de poliestireno, a adesão ocorreu geralmente de forma fraca. Os genes tadB, tadD, tadE e tadG, pertencentes ao locus tad, não apresentaram associação significativa com a produção de biofilme e nem com a origem de isolamento da cepa. Por fim, observou-se que as cepas de menor patogenicidade apresentaram uma maior capacidade de formação de biofilme em placas de poliestireno.(AU)

Establishment of a Pathogenicity Index for One-day-old Broilers to Pasteurella multocida Strains Isolated from Clinical Cases in Poultry and Swine

Although Pasteurella multocida is a member of the respiratory microbiota, under some circumstances, it is a primary agent of diseases , such as fowl cholera (FC), that cause significant economic losses. Experimental inoculations can be employed to evaluate the pathogenicity of strains, but the results are usually subjective and knowledge on the pathogenesis of this agent is still limited. The objective of this study was to establish a new methodology for classifying the pathogenicity of P. multocida by formulating a standard index. Strains isolated from FC cases and from swine with respiratory problems were selected. One hundred mL of a bacterial culture of each strain, containing 106 CFU, was inoculated in 10 one-day-old broilers. Mortality after inoculation, time of death (TD), and the presence of six macroscopic lesions were evaluated over a period of seven days post-inoculation (dpi). A Pathogenicity Index Per Bird (IPI), ranging 0 to 10, was calculated. Liver and heart fragments were collected to reisolate the bacteria. Blood was collected from the surviving birds, and an ELISA test was carried out to detect specific antibodies. The median of the pathogenicity indices, the number of lesions and the rate of bacteria reisolation were significantly different (p 0.05) among the origins of the isolates (p 0.05). The pathogenicity index developed in this study allows the classification of Pasteurella multocida pathogenicity and may be an alternative to the pathogenicity models currently used for screening.

Establishment of a Pathogenicity Index for One-day-old Broilers to Pasteurella multocida Strains Isolated from Clinical Cases in Poultry and Swine

Although Pasteurella multocida is a member of the respiratory microbiota, under some circumstances, it is a primary agent of diseases , such as fowl cholera (FC), that cause significant economic losses. Experimental inoculations can be employed to evaluate the pathogenicity of strains, but the results are usually subjective and knowledge on the pathogenesis of this agent is still limited. The objective of this study was to establish a new methodology for classifying the pathogenicity of P. multocida by formulating a standard index. Strains isolated from FC cases and from swine with respiratory problems were selected. One hundred mL of a bacterial culture of each strain, containing 106 CFU, was inoculated in 10 one-day-old broilers. Mortality after inoculation, time of death (TD), and the presence of six macroscopic lesions were evaluated over a period of seven days post-inoculation (dpi). A Pathogenicity Index Per Bird (IPI), ranging 0 to 10, was calculated. Liver and heart fragments were collected to reisolate the bacteria. Blood was collected from the surviving birds, and an ELISA test was carried out to detect specific antibodies. The median of the pathogenicity indices, the number of lesions and the rate of bacteria reisolation were significantly different (p 0.05) among the origins of the isolates (p 0.05). The pathogenicity index developed in this study allows the classification of Pasteurella multocida pathogenicity and may be an alternative to the pathogenicity models currently used for screening.(AU)

Virulence genes and antimicrobial resistance of Pasteurella multocida isolated from poultry and swine

Pasteurella multocida causes atrophic rhinitis in swine and fowl cholera in birds, and is a secondary agent in respiratory syndromes. Pathogenesis and virulence factors involved are still poorly understood. The aim of this study was to detect 22 virulence-associated genes by PCR, including capsular serogroups A, B and D genes and to evaluate the antimicrobial susceptibility of P. multocida strains from poultry and swine. ompH, oma87, plpB, psl, exbD-tonB, fur, hgbA, nanB, sodA, sodC, ptfA were detected in more than 90% of the strains of both hosts. 91% and 92% of avian and swine strains, respectively, were classified in serogroup A. toxA and hsf-1 showed a significant association to serogroup D; pmHAS and pfhA to serogroup A. Gentamicin and amoxicillin were the most effective drugs with susceptibility higher than 97%; however, 76.79% of poultry strains and 85% of swine strains were resistant to sulphonamides. Furthermore, 19.64% and 36.58% of avian and swine strains, respectively, were multi-resistant. Virulence genes studied were not specific to a host and may be the result of horizontal transmission throughout evolution. High multidrug resistance demonstrates the need for responsible use of antimicrobials in animals intended for human consumption, in addition to antimicrobial susceptibility testing to P. multocida. (AU)

Identification of the capsule type of Pasteurella multocida isolates from cases of fowl cholera by multiplex PCR and comparison with phenotypic methods

The ability of Pasteurella multocida to invade and multiply in its host is enhanced by the presence of the capsule, one of the most important virulence factors for this bacterium. Capsular typing methods are often used in epidemiological and pathogenesis studies of this agent. Five different serogroups have been identified based on serological typing. However, such tests are laborious, and agglutination of homologous antiserum may fail. The aim of this study was to develop a multiplex PCR protocol for the identification of the hyaD-hyaC and dcbF genes specific to serogroups A and D, respectively, and to compare these results with those of phenotypic tests for 54 strains isolated from fowl cholera cases in southern Brazil. The kappa coefficient and chisquare statistics were calculated to assess the agreement between the diagnostic methods and to determine the significance of the results, respectively. The multiplex PCR was able to detect the evaluated genes. Forty-nine strains (90.74%) were classified into serogroup A, and only two isolates (3.7%) were not identified as belonging to any of the serogroups analyzed. In contrast, with the phenotypic tests, only 41 strains (75.93%) were classified into serogroup A and 11 samples (20.37%) were unidentifiable. Of the strains analyzed, 70.37% were classified into the same serogroup (A) by both methods, and the kappa coefficient (k = 0.017) indicated poor agreement between the tests. Thus, multiplex PCR is an alternative for P. multocida capsular typing, as it allows the simultaneous and rapid detection of genes and also provides a greater strain-typing capacity.

Identification of the capsule type of Pasteurella multocida isolates from cases of fowl cholera by multiplex PCR and comparison with phenotypic methods

The ability of Pasteurella multocida to invade and multiply in its host is enhanced by the presence of the capsule, one of the most important virulence factors for this bacterium. Capsular typing methods are often used in epidemiological and pathogenesis studies of this agent. Five different serogroups have been identified based on serological typing. However, such tests are laborious, and agglutination of homologous antiserum may fail. The aim of this study was to develop a multiplex PCR protocol for the identification of the hyaD-hyaC and dcbF genes specific to serogroups A and D, respectively, and to compare these results with those of phenotypic tests for 54 strains isolated from fowl cholera cases in southern Brazil. The kappa coefficient and chisquare statistics were calculated to assess the agreement between the diagnostic methods and to determine the significance of the results, respectively. The multiplex PCR was able to detect the evaluated genes. Forty-nine strains (90.74%) were classified into serogroup A, and only two isolates (3.7%) were not identified as belonging to any of the serogroups analyzed. In contrast, with the phenotypic tests, only 41 strains (75.93%) were classified into serogroup A and 11 samples (20.37%) were unidentifiable. Of the strains analyzed, 70.37% were classified into the same serogroup (A) by both methods, and the kappa coefficient (k = 0.017) indicated poor agreement between the tests. Thus, multiplex PCR is an alternative for P. multocida capsular typing, as it allows the simultaneous and rapid detection of genes and also provides a greater strain-typing capacity.(AU)

Detection of virulence-associated genes of Pasteurella multocida isolated from cases of fowl cholera by multiplex-PCR / Pesquisa de genes associados à virulência em cepas de Pasteurella multocida isoladas em casos de cólera aviária através da técnica de multiplex-PCR

The current systems of breeding poultry, based on high population density, increase the risk of spreading pathogens, especially those causing respiratory diseases and those that have more than one host. Fowl Cholera (FC) is one such pathogen, and even though it represents one of several avian diseases that should be considered in the differential diagnosis of notifiable diseases that present with sudden death, the pathogenesis and virulence factors involved in FC are still poorly understood. The objective of this study was to investigate twelve genes related to virulence in 25 samples of Pasteurella multocida isolated from FC cases in the southern region of Brazil through the development of multiplex PCR protocols. The protocols developed were capable of detecting all of the proposed genes. The ompH, oma87, sodC, hgbA, hgbB, exBD-tonB and nanB genes were present in 100% of the samples (25/25), the sodA and nanH genes were present in 96% (24/25), ptfA was present in 92% (23/25), and pfhA was present in 60% (15/25). Gene toxA was not identified in any of the samples studied (0/25). Five different genetic profiles were obtained, of which P1 (negative to toxA) was the most common. We concluded that the multiplex-PCR protocols could be useful tools for rapid and simultaneous detection of virulence genes. Despite the high frequency of the analyzed genes and the fact that all samples belonged to the same subspecies of P. multocida, five genetic profiles were observed, which should be confirmed in a study with a larger number of samples.(AU)

Os atuais sistemas de criação na avicultura, baseados na alta densidade populacional, aumentam os riscos de disseminação de patógenos, especialmente das doenças respiratórias e daquelas cujos agentes etiológicos possuam mais de um hospedeiro. A Cólera Aviária (CA) apresenta estas características e apesar de representar uma das patologias aviárias que deve ser considerada para o diagnóstico diferencial de enfermidades com notificação obrigatória que cursam com morte súbita, a patogenia e os fatores de virulência envolvidos na CA ainda estão pouco elucidados. O objetivo deste trabalho foi pesquisar doze genes associados à virulência em 25 amostras de Pasteurella multocida isoladas de casos de CA na região sul do Brasil através do desenvolvimento de protocolos de multiplex-PCR. Os protocolos de multiplex-PCR desenvolvidos foram capazes de detectar todos os genes propostos. Os genes ompH, oma87, sodC, hgbA, hgbB, exBD-tonB, nanB estiveram presentes em 100% das amostras (25/25). Os genes sodA e nanH em 96% (24/25), o gene ptfA em 92% (23/25) e o gene pfhA em 60% (15/25). O gene toxA não foi identificado em nenhuma das amostras pesquisadas (0/25). Foram obtidos cinco diferentes perfis genéticos, sendo P1 (negativo para o gene toxA) o mais comum. Com este trabalho, concluiu-se que os protocolos de multiplex-PCR desenvolvidos tornam-se uma ferramenta bastante útil e rápida para a detecção simultânea dos genes de virulência. Apesar da alta frequência dos genes estudados e de todas as amostras pertencerem à mesma subespécie de P. multocida, foram observados cinco perfis genéticos, os quais devem ser confirmados em um estudo com um maior número de amostras.(AU)

ESTABELECIMENTO DE UM ÍNDICE DE PATOGENICIDADE EM CAMUNDONGOS PARA CEPAS DE Pasteurella multocida ISOLADAS DE AVES E SUÍNOS

Entre as doenças que podem trazer prejuízos à avicultura brasileira, destaca-se a cólera aviária (CA), uma doença contagiosa resultante da infecção pela bactéria Pasteurella multocida. Outras importantes enfermidades causadas pelo agente são a rinite atrófica progressiva em suínos, septicemia hemorrágica em bovinos e búfalos e pasteurelose em coelhos. Infecções em humanos parecem não ser tão frequentes, entretanto casos associados principalmente a mordeduras e/ou arranhaduras de cães e gatos já foram relatados. P. multocida está amplamente distribuída entre as espécies animais, mas pouco se conhece sobre a patogênese e especificidade a diversos hospedeiros. Muitos dados gerados a partir de metodologias de avaliação de patogenicidade podem ser subjetivos e pouco mensuráveis, pois geralmente envolvem apenas a observação da capacidade letal do agente em inoculações experimentais. Devido à falta de dados mais consistentes, o presente trabalho teve como objetivo estabelecer um modelo de classificação da patogenicidade de P. multocida isolada de aves e suínos, através da inoculação em camundongos. Foram utilizadas 94 cepas de P. multocida originárias de casos de cólera aviária e pulmões de suínos ao abate. Um volume de 0,1 mL obtido da concentração de 10 6 UFC/mL de cada isolado foi inoculado por via intraperitoneal nos camundongos. O período de observação, estabelecido a cada 6 horas, foi um critério importante na determinação de índices de patogenicidade (IPs) mais ajustados. Além da mortalidade observada neste período, outras variáveis foram consideradas, como o tempo de morte e as lesões macroscópicas. Os IPs obtidos apresentaram diferença significativa (p<0,05) conforme a origem das cepas. Da mesma forma, o número de lesões macroscópicas observadas e o percentual de isolamento foram distintos (p<0,05) entre as cepas de aves e de suínos. A partir dos índices observados, os isolados foram agrupados em três classes de patogenicidade: alta, média e baixa. O estudo propôs uma metodologia consistente de mensuração e classificação da patogenicidade de P. multocida e os resultados obtidos servirão para gerar outros modelos mais ajustados, bem como base para o diagnóstico da doença.

Among the diseases that can bring harm to the Brazilian poultry industry, there is Fowl Cholera (FC), a contagious disease resulting from infection by the bacterium Pasteurella multocida. Other important diseases caused by the agent are progressive atrophic rhinitis in swine, haemorrhagic septicemia in cattle and buffalo, and pasteurellosis in rabbits. The infections in humans do not appear so frequently, however the cases mainly associated with bite and/or scratching of dogs and cats have been reported. P. multocida is extensively distributed among animal species, but little is known about the pathogenesis and specificity to various hosts. Many reported data generated from pathogenicity evaluation methods can be subjective and little measurable, because usually only involve the observation of the lethal capacity of the agent in experimental inoculation. Due to lack of more consistent data, this study aims to establish a classification model of P. multocida pathogenicity that is isolated from poultry and swine by inoculation of mice. There were used 94 strains of P. multocida originating from fowl cholera and slaughter swine lungs. A volume of 0.1 mL obtained from the concentration of 10 6 UFC/mL was inoculated by intraperitoneally route in five mice. The observation period established every six hours was an important criterion in determining pathogenicity index (PIs), further adjusted. In addition to the mortality observed in this period, other variables were considered as the time of death and gross lesions. The PIs obtained showed significant differences (p <0,05) according to the origin of the strains. Likewise, the number of gross lesions and isolation percentages were different (p <0,05) among strains of poultry and swine. From the observed ratios, the isolates were grouped into three pathogenicity classes: high, medium and low. This study has proposed a consistent measurement and classification of P. multocida pathogenicity and the obtained results will be used to generate other adjusted models f, as well as the basis for disease diagnosis.

Caracterização fenotípica e molecular de cepas de Pasteurella multocida

Entre as bactérias que habitam a cavidade oral e nasal dos animais, os constituintes da família Pasteurellaceae estão entre os microrganismos comensais ou oportunistas mais prevalentes. Apesar do número de doenças associadas e da diversidade de hospedeiros acometidos, o conhecimento sobre a patogenia desta bactéria ainda é restrito. Além disto, a análise da virulência de Pasteurella multocida, que ocasiona casos agudos e crônicos de cólera aviária, não é comum. Tais estudos são ainda mais raros para cepas circulantes no Brasil. O objetivo deste trabalho foi a caracterização fenotípica e molecular de 96 cepas de P. multocida isoladas de aves e de suínos no país. As subespécies e os biovares foram determinados através de testes bioquímicos, e os sorogrupos foram classificados pelo emprego de testes fenotípicos não sorológicos. A susceptibilidade in vitro a nove antimicrobianos também foi avaliada. Para os estudos genotípicos, foi realizada a pesquisa de 22 genes de virulência por multiplex-PCR, incluindo-se aqueles determinantes dos sorogrupos, a comparação dos perfis genéticos e a diferenciação molecular através de PCR-RFLP a partir dos genes ompH e oma87. Por último, os testes fenotípicos e moleculares para classificação dos sorogrupos foram comparados, e a distribuição dos genes foi relacionada com índices de patogenicidade in vivo das cepas para a identificação de marcadores moleculares. Um total de 87,5% (84/96) das cepas foi classificado na subespécie multocida. O biovar 3 foi o mais comum entre as cepas aviárias e suínas, sendo identificado respectivamente em 35,7% (20/56) e 25% (10/40) dos casos. Entre as cepas aviárias, 90,7% (49/54) foram classificadas no sorogrupo A através do multiplex-PCR, e 3,7% (2/54) não foram classificados em um dos dois sorogrupos. Em contraste, somente 75,9% (41/54) das cepas aviárias foram identificadas no tipo capsular A através do teste fenotípico e 20,4% (11/54) não foram tipificadas. Resultados semelhantes foram observados entre os isolados suínos. As taxas de susceptibilidade das cepas aviárias foram superiores a 80% para os antimicrobianos testados, com exceção à enrofloxacina e ao sulfafurazol. Somente amoxicilina, ciprofloxacina e gentamicina inibiram o crescimento de mais de 80% das cepas suínas. 8,9% (5/56) dos isolados de origem aviária e 37,5% (15/40) das cepas suínas foram multirresistentes. A maioria dos genes (ompH, oma87, psl, plpB, exbD-tonB, fur, hgbA, nanH, nanB, sodA, sodC, pmHAS, ptfA) apresentou uma frequência superior a 90% e distribuição regular, independentemente da origem. As cepas foram agrupadas em 33 perfis, sendo o perfil 1 (toxA-; pfhA-; dcbF-; bcbD-; hsf-1-) o mais frequente, identificado em 16,7% (16/96) dos casos. O PCR-RFLP a partir do gene ompH permitiu a classificação das cepas aviárias em sete grupos moleculares, sendo predominante o grupo II, identificado em 42,9% (24/56) das situações. A detecção do gene pfhA indica a presença de cepas de alta patogenicidade em aves, e em segundo lugar, de cepas intermediárias. Este estudo proveu a caracterização fenotípica e molecular de cepas de P. multocida isoladas de aves e de suínos no Brasil e os seus resultados possibilitam a distinção futura dos isolados aviários quanto à patogenicidade.

The constituents of the Pasteurellaceae family are among the most prevalent commensal microorganisms or opportunistic pathogens that inhabit the oral and nasal cavity of the animals. The knowledge of the pathogenesis of this bacterium is still restricted, despite the number of related diseases and diversity of affected hosts. Similarly, analysis of the virulence of Pasteurella multocida, that causes acute and chronic cases of fowl cholera, is not common. Such studies are even rarer for the circulating strains in Brazil. The present work aimed to the phenotypic and molecular characterization of ninety-six P. multocida strains isolated from poultry and swine in the country. The subspecies and biovars were determined through biochemical scheme and the serogroups or capsular types were classified by employing non-serologic phenotypic tests. Furthermore, the susceptbility to nine antimicrobial agents was evaluated. For genotypic studies, the investigation of twenty-two virulence genes by multiplex-PCR, including those that are serogroups determinants, the comparing of the genetic profiles and the molecular differentiation by PCR-RFLP from ompH e oma87 were performed. Finally, the results of phenotypic and molecular tests for classification of serogroups were compared and the distribution of genes was related to in vivo pathogenic indices of strains for identification of molecular markers. 87.5% (84/96) of the strains were classified in multocida subspecies. The biovar 3 was more common among avian and swine strains, identified respectively in 35.7% (20/56) and 25% (10/40) of cases. Among avian strains, 90.7% (49/54) were classified in serogroup A by multiplex-PCR and 3.7% (2/54) were not classified in one of two serogroups. In contrast, only 75.9% (41/54) of avian strains were identified in the capsular type A through phenotypic test and 20.4% (11/54) were not typed. Similar results were observed among swine isolates. The susceptibility rates of avian strains were above 80% for the tested antimicrobials, except to enrofloxacin and sulfafurazol. Only amoxicillin, gentamicin and ciprofloxacin inhibited the growth of more than 80% of the swine strains. 8.9% (5/56) of avian isolates and 37.5% (15/40) of swine strains were multidrug-resistant. The majority of genes (ompH, oma87, psl, plpB, exbD-tonB, fur, hgbA, nanH, nanB, sodA, sodC, pmHAS, ptfA) had a frequency higher than 90% and regular distribution, regardless of source. The strains were grouped in 33 profiles and profile 1 (toxA-; pfhA-; dcbF-; bcbD-; hsf-1-) was most frequent, identified in 16.7% (16/96) of cases. The PCR-RFLP from ompH gene allowed the classification of avian strains in seven molecular groups. The predominant group II was identified in 42.9% (24/56) of cases. The detection of pfhA gene indicates the presence of highly pathogenic avian strains, and secondly, of intermediate strains. This study provided the phenotypic and molecular characterization of P. multocida isolated from poultry and swine in Brazil and its results enable future distinction of avian strains according the pathogenicity.